Canonical Allele Identifier: CA2160932247
Gene: ADSS1 HGNC NCBI

Linked Data

dbSNP Id: rs1470268018

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741031G>C , CM000676.2:g.104741031G>C GRCh38
NC_000014.8:g.105207368G>C , CM000676.1:g.105207368G>C GRCh37
NC_000014.7:g.104278413G>C NCBI36
NG_051175.1:g.21835G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710323.1:c.667-86G>C ENSP00000518203.1:n.667-86G>C
ENST00000330877.7:c.667-86G>C MANE Select ENSP00000331260.2:n.667-86G>C
ENST00000330877.6:c.667-86G>C ENSP00000331260.2:n.667-86G>C
ENST00000332972.9:c.796-86G>C ENSP00000333019.5:n.796-86G>C
ENST00000553540.5:c.779-86G>C ENSP00000450759.1:n.779-86G>C
ENST00000555486.5:c.732-86G>C ENSP00000473778.1:n.732-86G>C
ENST00000557582.5:n.1588-86G>C
NM_152328.3:c.667-86G>C NP_689541.1:n.667-86G>C
NM_199165.1:c.796-86G>C NP_954634.1:n.796-86G>C
XM_006720026.2:c.670-86G>C XP_006720089.1:n.670-86G>C
XM_011536412.1:c.799-86G>C XP_011534714.1:n.799-86G>C
XM_011536413.1:c.484-86G>C XP_011534715.1:n.484-86G>C
XM_011536414.1:c.481-86G>C XP_011534716.1:n.481-86G>C
XM_011536415.1:c.52-86G>C XP_011534717.1:n.52-86G>C
NM_001320424.1:c.52-86G>C NP_001307353.1:n.52-86G>C
NM_152328.4:c.667-86G>C NP_689541.1:n.667-86G>C
NM_199165.2:c.796-86G>C NP_954634.1:n.796-86G>C
XM_006720026.3:c.670-86G>C XP_006720089.1:n.670-86G>C
XM_011536412.2:c.799-86G>C XP_011534714.1:n.799-86G>C
NM_152328.5:c.667-86G>C MANE Select NP_689541.1:n.667-86G>C